Disease: Acute Chest Syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs6922269
rs6922269
Entrez Id: 25902
Gene Symbol: MTHFD1L
MTHFD1L
CUI: C0742343
Disease:
Acute Chest Syndrome 		0.020 GeneticVariation BEFREE We conclude, that rs6922269 variant at MTHFD1L gene could be an important prognostic factor for cardiovascular mortality in patients after ACS. 25809277 2015
dbSNP: rs6922269
rs6922269
Entrez Id: 25902
Gene Symbol: MTHFD1L
MTHFD1L
CUI: C0742343
Disease:
Acute Chest Syndrome 		0.020 GeneticVariation BEFREE After Cox adjustment for other ACS risk factors, of 95 SNPs tested in 811 whites only the association with the rs6922269 in MTHFD1L was statistically significant, with a 2.6-fold mortality hazard (P = 0.007). 21957892 2011